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Caffey Disease in Infancy: A diagnostic dilemma for primary care physicians
Caffey disease is a rare and self-limiting condition characterised by cortical hyperostosis with inflammation of adjacent fascia and muscles. It usually presents in infancy and clinical features include hyperirritability, acute inflammation with swelling of overlying soft tissues and subperiosteal n...
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| Veröffentlicht in: | Sultan Qaboos Univ Med J |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7065700/ https://ncbi.nlm.nih.gov/pubmed/32190379 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18295/squmj.2020.20.01.017 |
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